Photocatalytic C–H silylation of heteroarenes by using trialkylhydrosilanes

摘要

The efficient and selective C–H silylation of heteroarenes, especially the pharmaceutically relevant electron-deficient heteroarenes, represents a great challenge in organic synthesis. Herein we wish to report a distinctive visible light-promoted photocatalytic C–H silylation approach that enables the direct coupling of trialkylhydrosilanes with both electron-deficient and -rich heteroarenes as well as with cyano-substituted arenes in moderate to high yields and with good regioselectivity. The protocol features operational simplicity, mild reaction conditions, and the use of safe and readily available Na _(2) S _(2) O _(8) , bis(trimethylsilyl) peroxide (BTMSPO) or ~(i) Pr _(3) SiSH as the radical initiators. Notably, the challenging bulky and inert trialkylhydrosilanes, such as ( t -butyldimethyl)silane ( ~( t ) BuMe _(2) SiH) and (triisopropyl)silane ( ~(i) Pr _(3) SiH), work smoothly with the protocol. Moreover, despite the higher stability of ~( t ) BuMe _(2) Si silylation products, our studies revealed their great reactivity and versatility in diverse C–Si-based chemical transformations, providing an operationally simple, low-cost, and environmentally benign synthetic technology for molecule construction and elaboration.